Hereditary congenital myasthenic syndrome multigene analysis in Blood or Tissue by Molecular genetics method 103732-4
LOINC Code
LOINC code | 103732-4 | ||
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name | Hereditary congenital myasthenic syndrome multigene analysis in Blood or Tissue by Molecular genetics method | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Hereditary congenital myasthenic syndrome multigene analysis | ||
property | Find = Finding | ||
time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
system | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
short name | Hrd cong mya synd multi Bld/T | ||
Basic Attributes | |||
class | MOLPATH | ||
type | 1 Laboratory | ||
order vs. observation | Both | ||
Ask At Order Entry | |||
Ask at Order Entry (AOE) observations for a clinical observation or laboratory test. A LOINC term may represent a single AOE observation or a panel containing several AOE observations.
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Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
first released | |||
last updated | 2.77 | ||
last change type | ADD - added | ||
Related Names | |||
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